ClinVar Miner

Submissions for variant NM_153717.3(EVC):c.802-12_802-11del

dbSNP: rs372546602
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001649911 SCV001868274 benign not provided 2019-08-11 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002488443 SCV002799344 benign Ellis-van Creveld syndrome; Curry-Hall syndrome 2022-04-21 criteria provided, single submitter clinical testing

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